Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: Neural Tube Defects and MTRR[original query] |
---|
The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations. Atherosclerosis 2001 Aug 157 (2): 451-6. Gaughan DJ, Kluijtmans LA, Barbaux S, McMaster D, Young IS, Yarnell JW, Evans A, Whitehead AS |
Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Molecular genetics and metabolism 2003 Mar 78 (3): 216-21. Zhu Huiping, Wicker Ned J, Shaw Gary M, Lammer Edward J, Hendricks Kate, Suarez Lucina, Canfield Mark, Finnell Richard |
Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. Blood 2003 Apr 101 (7): 2483-8. Kluijtmans Leo A J, Young Ian S, Boreham Colin A, Murray Liam, McMaster Dorothy, McNulty Helene, Strain J J, McPartlin Joseph, Scott John M, Whitehead Alexander |
Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population. Journal of medical genetics 2004 Apr 41 (4): 256-60. Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, Tawn EJ, Burn J |
Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association. Molecular genetics and metabolism 2005 Jul 85 (3): 220-7. O'Leary Valerie B, Mills James L, Pangilinan Faith, Kirke Peadar N, Cox Christopher, Conley Mary, Weiler Andrea, Peng Kun, Shane Barry, Scott John M, Parle-McDermott Anne, Molloy Anne M, Brody Lawrence C, |
Detection of MTRR 66A-->G polymorphism using the real-time polymerase chain reaction machine LightCycler for determination of composition of allele after restriction cleavage. Scandinavian journal of clinical and laboratory investigation 2006 66 (8): 685-93. Tvedegaard K C, Rüdiger N S, Pedersen B N, Møller |
Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: a multicenter case-control study. American journal of medical genetics. Part A 2008 May 146A (9): 1128-33. Candito Mirande, Rivet Romain, Herbeth Bernard, Boisson Catherine, Rudigoz René-Charles, Luton Dominique, Journel Hubert, Oury Jean-François, Roux François, Saura Robert, Vernhet Isabelle, Gaucherand Pascal, Muller Françoise, Guidicelli Béatrice, Heckenroth Hélène, Poulain Patrice, Blayau Martine, Francannet Christine, Roszyk Laurence, Brustié Cécile, Staccini Pascal, Gérard Philippe, Fillion-Emery Nathalie, Guéant-Rodriguez Rosa-Maria, Van Obberghen Emmanuel, Guéant Jean-Lou |
Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India. Journal of perinatal medicine 2010 38 (1): 63-9. Naushad Shaik Mohammad, Devi Akella Radha Ra |
Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: a meta-analysis. Gene 2012 Dec . Ouyang S, Li Y, Liu Z, Chang H, Wu J |
Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature. PloS one 2013 8 (4): e59570. Zhang Ti, Lou Jiao, Zhong Rong, Wu Jing, Zou Li, Sun Yu, Lu Xuzai, Liu Li, Miao Xiaoping, Xiong Guangli |
Meta-analyses on the association of MTR A2756G and MTRR A66G polymorphisms with neural tube defect risks in Caucasian children. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2013 Aug 26 (12): 1166-70. Ouyang Shengrong, Liu Zhuo, Li Yuanyuan, Wu Jianx |
"Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis". Metabolic brain disease 2015 Feb 30 (1): 7-24. Yadav Upendra, Kumar Pradeep, Yadav Sushil Kumar, Mishra Om Prakash, Rai Vanda |
Analysis of MTR and MTRR Polymorphisms for Neural Tube Defects Risk Association. Medicine 2015 Sep 94 (35): e1367. Wang Yongxin, Liu Yuan, Ji Wenyu, Qin Hu, Wu Hao, Xu Danshu, Tukebai Turtuohut, Wang Zenglia |
Functional variant in methionine synthase reductase intron-1 is associated with pleiotropic congenital malformations. Molecular and cellular biochemistry 2015 Sep 407 (1-2): 51-6. Cheng Haiqin, Li Huili, Bu Zhaoli, Zhang Qin, Bai Baoling, Zhao Hong, Li Ren-Ke, Zhang Ting, Xie J |
An Inframe Trinucleotide Deletion in MTRR Exon 1 is Associated with the Risk of Spina Bifida. Neuromolecular medicine 2017 Jul . Zhang Jun, Dai Xiao-Lu, Liu Gui-Cen, Wang Juan, Ren Xue-Yi, Jin Mu-Hua, Mi Nan-Nan, Wang Shu-Q |
Association of main folate metabolic pathway gene polymorphisms with neural tube defects in Han population of Northern China. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2018 Feb . Fang Yulian, Zhang Ruiping, Zhi Xiufang, Zhao Linsheng, Cao Lirong, Wang Yizheng, Cai Chunqu |
Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents. Pathobiology : journal of immunopathology, molecular and cellular biology 2019 Jun 1-11. Nasri Kaouther, Midani Fatma, Kallel Amani, Ben Jemaa Nadia, Aloui Mariem, Boulares Miryam, Lassoued Mehdi, Ben Halima Meriam, Ben Wafi Safa, Soussi Mariem, Mahjoubi Imen, Baara Abir, Ben Fradj Mohamed Kacem, Omar Souhail, Feki Moncef, Jemaa Riadh, Gaigi Soumeya Siala, Marrakchi Ra |
Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway. Italian journal of pediatrics 2019 Mar 45 (1): 37. Cai Chun-Quan, Fang Yu-Lian, Shu Jian-Bo, Zhao Lin-Sheng, Zhang Rui-Ping, Cao Li-Rong, Wang Yi-Zheng, Zhi Xiu-Fang, Cui Hua-Lei, Shi Ou-Yan, Liu W |
Structural insight into the effect of polymorphic variation on the functional dynamics of methionine synthase reductase: Implications in neural tube defects. Chemical biology & drug design 2020 8 97 (2): 283-292. Sadhukhan Susanta, Maity Subhajit, Chakraborty Sandipan, Paul Silpita, Munian Dinesh, Kumar Pattanayak Arup, Jana Biman, Das Madhusud |
[Geographical distribution characteristics of one carbon metabolic pathway related single nucleotide polymorphisms]. Wei sheng yan jiu = Journal of hygiene research 2020 4 49 (1): 123-131. Zhang Chunhong, Huo Junsheng, Sun Jing, Huang Ji |
Folate Pathway Gene Single Nucleotide Polymorphisms and Neural Tube Defects: A Systematic Review and Meta-Analysis. Journal of personalized medicine 2022 10 12 (10): . Almekkawi Ahmad K, AlJardali Marwa W, Daadaa Hicham M, Lane Alison L, Worner Ashley R, Karim Mohammad A, Scheck Adrienne C, Frye Richard |
Polymorphisms in Maternal Selected Folate Metabolism-Related Genes in Neural Tube Defect-Affected Pregnancy. Advanced biomedical research 2023 8 12 160. Winner K Dewelle, Daniel S Melka, Abenezer T Aklilu, Mahlet Y Gebremariam, Markos A Alemayehu, Dawit H Alemayehu, Tamrayehu S Woldemichael, Solomon G Geb |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
- Content source: